Detalhe da pesquisa
1.
Multi-layered effects of Panax notoginseng on immune system.
Pharmacol Res
; 204: 107203, 2024 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38719196
2.
Synthesis and biological evaluation of pyrazole-fused oleanolic acid derivatives as novel inhibitors of inflammatory and osteoclast differentiation.
Bioorg Med Chem
; 80: 117177, 2023 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36701870
3.
Detection and Mitigation of SYN Flooding Attacks through SYN/ACK Packets and Black/White Lists.
Sensors (Basel)
; 23(8)2023 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37112158
4.
Ru-Catalyzed Defluorinative Alkylation or Catalyst-Free Hydroalkylation of gem-Difluoroalkenes Enabled by Visible Light.
J Org Chem
; 87(5): 2730-2739, 2022 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35133834
5.
Design, synthesis and evaluation of the Brigatinib analogues as potent inhibitors against tertiary EGFR mutants (EGFRdel19/T790M/C797S and EGFRL858R/T790M/C797S).
Bioorg Med Chem Lett
; 72: 128729, 2022 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35413415
6.
Photoredox-catalysed regioselective synthesis of C-4-alkylated pyridines with N-(acyloxy)phthalimides.
Org Biomol Chem
; 20(9): 1969-1973, 2022 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35175267
7.
Identification of 2-substituted pyrrolo[1,2-b]pyridazine derivatives as new PARP-1 inhibitors.
Bioorg Med Chem Lett
; 31: 127710, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246105
8.
Synthesis of 2-alkyl-chroman-4-ones via cascade alkylation-dechlorination of 3-chlorochromones.
Org Biomol Chem
; 19(24): 5348-5352, 2021 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34042936
9.
Design, synthesis and antiproliferative activity evaluation of a series of pyrrolo[2,1-f][1,2,4]triazine derivatives.
Bioorg Med Chem Lett
; 30(12): 127194, 2020 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32317209
10.
Correction: Regioselective synthesis of substituted thiazoles via cascade reactions from 3-chlorochromones and thioamides.
Org Biomol Chem
; 18(47): 9726, 2020 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33237106
11.
Regioselective synthesis of substituted thiazoles via cascade reactions from 3-chlorochromones and thioamides.
Org Biomol Chem
; 18(31): 6162-6170, 2020 08 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32716017
12.
Comparison of three-dimensional printing guides and double-layer guide plates in accurate bracket placement.
BMC Oral Health
; 20(1): 127, 2020 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32345292
13.
Substituent-Oriented Synthesis of Substituted Pyrazoles/Chromeno[3,2- c]pyrazoles via Sequential Reactions of Chromones/3-Chlorochromones and Tosylhydrazones.
J Org Chem
; 84(9): 5913-5921, 2019 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30919626
14.
Convenient Synthesis of 6,7,12,13-Tetrahydro-5H-Cyclohepta[2,1-b:3,4-b']diindole Derivatives Mediated by Hypervalent Iodine (III) Reagent.
Molecules
; 24(5)2019 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30857232
15.
One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones.
Molecules
; 24(16)2019 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31434258
16.
C-H Trifluoromethylation of 2-Substituted/Unsubstituted Aminonaphthoquinones at Room Temperature with Bench-Stable (CF3SO2)2Zn: Synthesis and Antiproliferative Evaluation.
J Org Chem
; 82(13): 6795-6800, 2017 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28589724
17.
Corrigendum to "Identification of 2-substituted pyrrolo[1,2-b]pyridazine derivatives as new PARP-1 inhibitors" [Bioorg. Med. Chem. Lett. 31 (2021) 127710].
Bioorg Med Chem Lett
; 56: 128501, 2022 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34911648
18.
Feasibility of Shape-Memory Ni/Ti Alloy Wire Containing Tube Elevators for Transcrestal Detaching Maxillary Sinus Mucosa: Ex Vivo Study.
Cell Physiol Biochem
; 40(5): 944-952, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27941347
19.
An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes.
Org Biomol Chem
; 13(25): 6935-9, 2015 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26041017
20.
Efficient Pd-catalyzed domino synthesis of 1-phenyl-1H-indol-2-amine and 5-amino-indolo[1,2-a]quinazoline derivatives.
Org Biomol Chem
; 13(40): 10122-6, 2015 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26377704